Abstract

This unit describes a viral entry assay where a beta-lactamase reporter protein fused to the matrix protein of either influenza (BlaM1) or ebola virus (BlaVP40) is packaged as a structural component into virus-like particles (VLPs). The Bla reporter is released upon fusion with target cells and can be detected in live cells by flow cytometry, microscopy, or a fluorometric plate reader for utility in high-throughput screening approaches. The transfer of Bla to a target cell by BlaM1 or BlaVP40 VLPs requires the presence of influenza hemagglutinin (HA) and neuraminidase (NA) or EboV glycoprotein (GP), respectively. This straightforward assay has broad application for studying the entry steps of enveloped viruses, especially those that require high levels of biosafety containment.

Original languageEnglish
Article number26.12
JournalCurrent Protocols in Cell Biology
Issue numberSUPP.51
DOIs
StatePublished - Jun 2011

Keywords

  • Ebola virus
  • Flow cytometry
  • Influenza virus
  • Marburg virus
  • Microscopy
  • Virus entry

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